Variant report

Variant rs9536192
Chromosome Location chr13:53183139-53183140
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:53175000-53191000 Weak transcription Fetal Stomach stomach
2 chr13:53175200-53183200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
3 chr13:53175200-53183200 Weak transcription Stomach Smooth Muscle stomach
4 chr13:53181200-53190000 Weak transcription Monocytes-CD14+_RO01746 blood
5 chr13:53182200-53183200 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chr13:53182200-53183800 Enhancers HUVEC blood vessel
7 chr13:53182400-53183200 Enhancers HepG2 liver
8 chr13:53182400-53183600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr13:53182400-53186000 Enhancers Fetal Heart heart
10 chr13:53182600-53183400 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr13:53182800-53184400 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr13:53183000-53183200 Enhancers Lung lung
13 chr13:53183000-53183400 Enhancers Fetal Intestine Large intestine
14 chr13:53183000-53183600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr13:53183000-53183800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain

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